Galantamine
- Product NDC
- 72162-2566
- 11-digit product format
- 721622566
- Labeler code
- 72162
- Product ID
- 72162-2566_cf937559-bf6e-4dfd-b651-7b8fcb839e36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Galantamine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090957
- Marketing category
- ANDA
- Marketing start
- 2011-03-29
- Substance
- GALANTAMINE HYDROBROMIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Galantamine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GALANTAMINE HYDROBROMIDE | 8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MJ4PTD2VVW |
| Rxcui | 310437 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2566-6 | Galantamine | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2566-6 | 72162256606 | 60 TABLET, FILM COATED in 1 BOTTLE (72162-2566-6) | 2025-11-04 | No | No | Current |